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7.88J Protein Folding ProblemFall 2007

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Coiled Coils

7.88J Protein Folding

Prof. David Gossard

September 24, 2003

PDB Acknowledgements

The Protein Data Bank (PDB - http://www.pdb.org/) is the single worldwide repository for the processing and distribution of 3-D biological macromolecular structure data.

Berman, H. M., J. Westbrook, Z. Feng, G. Gilliland, T. N. Bhat, H.Weissig, I. N.Shindyalov, and P. E.Bourne. “The Protein Data Bank.” Nucleic Acids Research 28 (2000): 235-242.

(PDB Advisory Notice on using materials available in the archive: http://www.pdb.org/pdb/static.do?p=general_information/about_pdb/pdb_advisory.html )

PDB molecules and citations used in the “Coiled Coils” Lecture Notes for 7.88J - Protein Folding

PDB ID: 2ZTA

JRNL reference: O'Shea, E. K., J. K. Klemm, P. S. Kim., and T. Alber. “X-ray structure of the GCN4 leucine zipper, a two-

stranded, parallel coiled coil.” Science 254 (1991): 539.

Pages: 3 (“Outline”), 14-15 (“GCN4 Leucine Zipper”)

Outline

• Review Key Features of Coiled Coils

• Examine a Particular Example

– GCN4 Leucine Zipper (2ZTA)

C

Coiled Coils

• Left-handed spiral of right-handed helices

• May be parallel

N

N C

C

or anti-parallel

N C

N

2-Stranded Coiled Coils

• GCN4

• Tropomyosin

• Intermediate

filament protein

• Lamin

• M-protein

• Paramyosin

• Myosin

Crick’s Models

• Geometry of Helix (Coil)

x y

z t

roP

Zo

Z > 0 right-handed oR(t)

x(t) = r cos(o Z t)o

y(t) = r sin(o Z t)o

z(t) = P (Z t /2o S)

= tan r0 0

Crick, F. H. C. “The Fourier Transform of a Coiled-coil.”

Acta Cryst 6 (1953): 685-689.

x y

Geometry of Coiled-CoilMinor

ro t

r1

helix z'z t

Z < 0 Major axis y' o left-handed

x' Minor axis Z1 > 0

right-handed

Major yhelix

x(t) = r0 cos Z t + r cos Z0t cos Z t - r cos D sin Z0t sin Z t0 1 1 1 1

y(t) = r0 sin Z t + r sin Z t cos Z t + r cos D cos Z t sin Z t0 1 0 1 1 0 1

z(t) = p0(Z0t) - r1sin D sin Z t1

D –1 (2S /p )

z

x

be -/+

Figure adapted from Cohen, et.al., PROTEINS: Structure, Function and Genetics 7:1-15 (1990)

Features of Coiled Coil

• Heptad repeat in sequence

– [a b c d e f g]n

• Hydrophobic residues at “a” and “d”

• Charged residues at “e” and “g”

a

c

f

g

d

+/-Charged

residues at

“e” and “g”Hydrophobic

residues at

“a” and “d”

eg + -

Figure adapted from Cohen, et.al., PROTEINS: Structure, Function and Genetics 7:1-15 (1990)

Significance of Heptad Repeat• Hydrophobic residues at “a” and “d”

– form hydrophobic core with other coil

• Charged residues at “e” and “g”

– form ion pairs with oppositely charged residues on other coil

– may distinguish parallel from anti-parallel coiled coils

a b

cd

f

g

a

d

e b

c

+-

f

Hydrophobic residues

Heptad Repeat in 3D

a

b

c

d

e f g

a b

cd

e

f

g

Charged

residues+/­

-/+

+/­ -/+

Hydrophobic Core is on Axis of

Superhelix ( ~Straight)

d

d a

a

Charged Residues Provide Stability, Registration

Charged residues

“e” and “g”

Ion pairs

between

coils

Figure adapted from Crick, F. H. C. “The Packing of D-helices: Simple Coiled-

coils.” Acta Cryst. 6 (1953): 689-697.

“Knobs in Holes” Packing

“about 20°…” Helix axis

GCN4 Leucine Zipper (2ZTA)

• Parallel Coiled Coil

• Major helix pitch ~ 180 A/turn

• 8 turns

• 31 residues

O’Shea, Erin, Juli D. Klemm, Peter S. Kim, and Tom Alber,

“X-ray S tructure of the GCN4 Leucine Zipper, a Two-Stranded,

Parallel Coiled Coil.” Science 254 (October 25, 1991): 539-544.

– Glu22’ – Lys27

GCN4 Leucine Zipper (2ZTA)

•

• 15 20’

22 27’

a b c d e f g

Residues contain heptad repeat

Ion pairs

– Lys – Glu

– Glu – Lys

ARG1 MET2 LYS3 GLN4 LEU5 GLU6 ASP7 LYS8

VAL9 GLU10 GLU11 LEU12 LEU13 SER14 LYS15

ASN16 TYR17 HIS18 LEU19 GLU20 ASN21 GLU22

VAL23 ALA24 ARG25 LEU26 LYS27 LYS28 LEU29

VAL30 GLY31

Crossing Angle ~18o

Molecular Surface of GCN4

3D Demonstrations

• Tour of Heptad Repeat (3D Studio MAX)

• Tour of GCN4 (Swiss-PDB)

3 & 4-Stranded Coiled Coils

• 3-stranded – Gp17 (T7)

– Fibrinogen (heterotrimer)

– GCN4 mutant

• 4-stranded parallel – GCN4 mutants

• 4-stranded anti-parallel – Myohaemerythrin

– Tobacco mosaic virus

– Cytochrome c’

– Apoferritin

b f

eFigure adapted from Cohen, C., and D.A. D. Perry, “D-helical

coiled coils and bundles: How to design an D-helical protein.”

PROTEINS: Structure, Function, and Genetics 7 (1990): 1-15.

3-Stranded Coiled Coil!?

(parallel)

• Axial symmetry

• Hydrophobic core

• Ion pairs a

b

c d

e

f

g a

d g

a

b

c

d e

f

g

c

b c

f

Figure adapted from Cohen, C., and D.A.D. Perry, “D-helical

coiled coils and bundles: How to design an D-helical protein.”

PROTEINS: Structure, Function, and Genetics 7 (1990): 1-15.

4-Stranded Coiled Coil!?

(parallel)

• Axial symmetry

• Hydrophobic core

• Ion pairs a

b

c d

e

f

g

a

b

d

e

f

g

a d

e g

a

bc

d

e

f

g

c

Harbury, P. B., Tao Zhang, Peter S. Kim, and Tom Alber.

“A Switch Between Two-, Three-, and Four-Stranded Coiled Coils

in GCN4 Leucine Zipper Mutants.” Science 262 (1993): 1401-1407.

Recall - GCN4

• Hydrophobic core:

“a” (blue) “d” (red)

Val9 Leu5

Asn16 Leu12

Val23 Leu19

Val30 Leu26

Mutagenized Hydrophobic Core

• p-LI ( X => Leu - volume-preserving)

“a” “d”

Leu9 Ile5

Leu16 Ile12

Leu23 Ile19

Leu30 Ile26

• => tetramer (parallel) !!

Mutant p-LI

P-LIGCN4

b c

f

GCN4 p-LI

• Ion pairs/salt bridges

– ‘e’ & ‘g’ (5/12)

• GluB6 – ArgA1

– ‘g’ & ‘b’ (4/8)

• LysD8 – GluA10

– ‘e’ & ‘c’ (5/8)

• HisB18 – GluC20

a b

c d

e

f

g

a

b

d

e

f

g

a d

e g

a

bc

d

e

f

g

c